GapMind for catabolism of small carbon sources

 

Alignments for a candidate for nagX in Shewanella loihica PV-4

Align DUF5009 domain-containing protein (characterized, see rationale)
to candidate 5208607 Shew_1118 hypothetical protein (RefSeq)

Query= uniprot:A0KZW6
         (395 letters)



>FitnessBrowser__PV4:5208607
          Length = 387

 Score =  567 bits (1460), Expect = e-166
 Identities = 273/378 (72%), Positives = 311/378 (82%), Gaps = 5/378 (1%)

Query: 23  KRQSKPRLMSLDALRGFDMFWILGGEALFGALLMLTGWAGWQWGDTQMHHSEWNGFRFYD 82
           K  +KPRLMSLDALRGFDMFWILGGEALF ALL+ TGW GW+  D QMHHS+W+GF FYD
Sbjct: 10  KPAAKPRLMSLDALRGFDMFWILGGEALFAALLVWTGWQGWRIADAQMHHSQWHGFTFYD 69

Query: 83  LIFPLFIFLSGVALGLSPKRLDKLPMQERMPVYRHGIKRLFLLLLLGILYNHGWGTGAPA 142
           LIFPLFIFLSGVALGLSPKRLD LP  ER+P+YRH IKRL LLLL G+LYNHGWGTG P 
Sbjct: 70  LIFPLFIFLSGVALGLSPKRLDSLPWPERLPLYRHAIKRLMLLLLFGVLYNHGWGTGMPM 129

Query: 143 DPEKVRYASVLGRIAFAWFFAALLVWHTSLRTQVLVALGILVAYGAVQLWLPFPGGQAGV 202
             ++VRYASVLGRIAFAWFFAALLVWHT L+TQ+LVA+GIL+ Y A+QLWLP PGG AG 
Sbjct: 130 AADEVRYASVLGRIAFAWFFAALLVWHTDLKTQILVAIGILLGYAAMQLWLPVPGGVAGD 189

Query: 203 LSPTESINAYVDSLLLPGVSYQGRTPDPEGVLSTLPAVVNALAGVFVGHFIVKSHP---- 258
            S + SINAYVD   LPG+SYQGR  DPEG+LSTLPA+VNALAGVF G FIVKSHP    
Sbjct: 190 FSISGSINAYVDGKFLPGISYQGRATDPEGILSTLPAIVNALAGVFTGRFIVKSHPKWGG 249

Query: 259 -KGEWAKVGLLSVAGGVCLALGWLLGGVIPVNKELWTSSFVLVTSGWSMLLLALFYALVD 317
            KGEWAKVG+L +AG + L LGWL+   IPVNK+LWTSSFV+VT GWS++LLA+FYALVD
Sbjct: 250 VKGEWAKVGILLLAGLLSLGLGWLMNPYIPVNKDLWTSSFVMVTLGWSLILLAIFYALVD 309

Query: 318 VLKWQKLAFIFVVIGTNAIIIYLASSLVDWKYIAQSVFGGVIAVLPENAQPLGAVIGLLT 377
           VLK  +LAF FVVIG NAIIIYLASSLV W Y+A S+FGG I  LP   QPL +   +L 
Sbjct: 310 VLKLHRLAFGFVVIGCNAIIIYLASSLVKWDYLASSLFGGAIQALPIEMQPLASACAMLL 369

Query: 378 VQWLVLYWMYRRNIFVRI 395
           VQWL+LYWMY+R IF+++
Sbjct: 370 VQWLLLYWMYKRGIFIKV 387


Lambda     K      H
   0.326    0.141    0.457 

Gapped
Lambda     K      H
   0.267   0.0410    0.140 


Matrix: BLOSUM62
Gap Penalties: Existence: 11, Extension: 1
Number of Sequences: 1
Number of Hits to DB: 723
Number of extensions: 34
Number of successful extensions: 3
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 1
Number of HSP's successfully gapped: 1
Length of query: 395
Length of database: 387
Length adjustment: 31
Effective length of query: 364
Effective length of database: 356
Effective search space:   129584
Effective search space used:   129584
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 15 ( 7.0 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 40 (21.6 bits)
S2: 50 (23.9 bits)

This GapMind analysis is from Sep 17 2021. The underlying query database was built on Sep 17 2021.

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About GapMind

Each pathway is defined by a set of rules based on individual steps or genes. Candidates for each step are identified by using ublast (a fast alternative to protein BLAST) against a database of manually-curated proteins (most of which are experimentally characterized) or by using HMMer with enzyme models (usually from TIGRFam). Ublast hits may be split across two different proteins.

A candidate for a step is "high confidence" if either:

where "other" refers to the best ublast hit to a sequence that is not annotated as performing this step (and is not "ignored").

Otherwise, a candidate is "medium confidence" if either:

Other blast hits with at least 50% coverage are "low confidence."

Steps with no high- or medium-confidence candidates may be considered "gaps." For the typical bacterium that can make all 20 amino acids, there are 1-2 gaps in amino acid biosynthesis pathways. For diverse bacteria and archaea that can utilize a carbon source, there is a complete high-confidence catabolic pathway (including a transporter) just 38% of the time, and there is a complete medium-confidence pathway 63% of the time. Gaps may be due to:

GapMind relies on the predicted proteins in the genome and does not search the six-frame translation. In most cases, you can search the six-frame translation by clicking on links to Curated BLAST for each step definition (in the per-step page).

For more information, see:

If you notice any errors or omissions in the step descriptions, or any questionable results, please let us know

by Morgan Price, Arkin group, Lawrence Berkeley National Laboratory